CN110268544A - 有机电致发光器件 - Google Patents
有机电致发光器件 Download PDFInfo
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- CN110268544A CN110268544A CN201880008450.1A CN201880008450A CN110268544A CN 110268544 A CN110268544 A CN 110268544A CN 201880008450 A CN201880008450 A CN 201880008450A CN 110268544 A CN110268544 A CN 110268544A
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- organic electroluminescence
- aromatics
- electroluminescence device
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- 238000005401 electroluminescence Methods 0.000 title claims abstract description 43
- 238000002347 injection Methods 0.000 claims abstract description 42
- 239000007924 injection Substances 0.000 claims abstract description 42
- 238000004519 manufacturing process Methods 0.000 claims abstract description 11
- 150000004696 coordination complex Chemical class 0.000 claims abstract description 8
- 125000003118 aryl group Chemical group 0.000 claims description 63
- 125000000217 alkyl group Chemical group 0.000 claims description 29
- 125000004432 carbon atom Chemical group C* 0.000 claims description 29
- 150000001875 compounds Chemical class 0.000 claims description 26
- 230000005540 biological transmission Effects 0.000 claims description 25
- 229910052797 bismuth Inorganic materials 0.000 claims description 22
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 22
- 229910052731 fluorine Inorganic materials 0.000 claims description 22
- 229910052760 oxygen Inorganic materials 0.000 claims description 22
- 125000001072 heteroaryl group Chemical group 0.000 claims description 21
- 229910052717 sulfur Inorganic materials 0.000 claims description 19
- 125000005259 triarylamine group Chemical group 0.000 claims description 19
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 18
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- 125000004122 cyclic group Chemical group 0.000 claims description 16
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 15
- 229910052733 gallium Inorganic materials 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 15
- 125000003545 alkoxy group Chemical group 0.000 claims description 12
- 125000005842 heteroatom Chemical group 0.000 claims description 11
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- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 9
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 8
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- 229910052794 bromium Inorganic materials 0.000 claims description 8
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- 125000004475 heteroaralkyl group Chemical group 0.000 claims description 8
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- 125000001424 substituent group Chemical group 0.000 claims description 7
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- IZRTVYMPRPTBAI-UHFFFAOYSA-K dibenzoyloxybismuthanyl benzoate Chemical compound [Bi+3].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 IZRTVYMPRPTBAI-UHFFFAOYSA-K 0.000 claims description 3
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- 125000003277 amino group Chemical group 0.000 claims 1
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- CYSPWCARDHRYJX-UHFFFAOYSA-N 9h-fluoren-1-amine Chemical compound C12=CC=CC=C2CC2=C1C=CC=C2N CYSPWCARDHRYJX-UHFFFAOYSA-N 0.000 description 7
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- 239000012044 organic layer Substances 0.000 description 6
- DXBHBZVCASKNBY-UHFFFAOYSA-N 1,2-Benz(a)anthracene Chemical compound C1=CC=C2C3=CC4=CC=CC=C4C=C3C=CC2=C1 DXBHBZVCASKNBY-UHFFFAOYSA-N 0.000 description 5
- 101100489923 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) ABF2 gene Proteins 0.000 description 5
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- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 4
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 4
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 4
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- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 4
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Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/94—Bismuth compounds
-
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EP3462516A1 (en) * | 2017-10-02 | 2019-04-03 | Novaled GmbH | Electronic device and method for preparing the same |
EP3790857B1 (en) | 2019-06-28 | 2023-01-11 | Idemitsu Kosan Co., Ltd. | Compound, material for organic electroluminescence element, organic electroluminescence element and electronic device |
WO2021214348A2 (de) * | 2020-10-09 | 2021-10-28 | Merck Patent Gmbh | Verbindungen für elektronische vorrichtungen |
EP4152425A1 (en) * | 2021-09-20 | 2023-03-22 | Novaled GmbH | An organic electronic device comprising a substrate, an anode layer, a cathode layer, at least one first emission layer, and a hole injection layer, wherein the hole injection layer comprises a metal complex of formula (i) and a compound of formula (ii), wherein the hole injection layer is arranged between the anode layer and the at least one first emission layer |
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KR20230170828A (ko) | 2023-12-19 |
KR20190126097A (ko) | 2019-11-08 |
CN117440703A (zh) | 2024-01-23 |
US11393987B2 (en) | 2022-07-19 |
JP2020511006A (ja) | 2020-04-09 |
WO2018158232A1 (en) | 2018-09-07 |
EP3590141A1 (en) | 2020-01-08 |
US20190372025A1 (en) | 2019-12-05 |
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